Canonical Allele Identifier: CA528080527
Gene: PTGS2 HGNC NCBI

Linked Data

dbSNP Id: rs1365603857
gnomAD v2: 1-186649722-A-C
gnomAD v3: 1-186680590-A-C
gnomAD v4: 1-186680590-A-C
MyVariant Identifiers: chr1:g.186649722A>C (hg19) chr1:g.186680590A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680590A>C , CM000663.2:g.186680590A>C GRCh38
NC_000001.10:g.186649722A>C , CM000663.1:g.186649722A>C GRCh37
NC_000001.9:g.184916345A>C NCBI36
NG_028206.2:g.4838T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000680451.1:c.-114+114T>G ENSP00000506242.1:n.-114+114T>G
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